FDA Inspection 1023505 — Steripack Usa Limited Llc
The FDA completed an inspection of Steripack Usa Limited Llc on August 4, 2017 in Lakeland, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- August 4, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Lakeland, FL (United States)